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https://hdl.handle.net/2440/4904
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Type: | Journal article |
Title: | Aryl nitrile oxide cycloaddition reactions in the presence of baker's yeast and β-cyclodextrin |
Other Titles: | Aryl nitrile oxide cycloaddition reactions in the presence of baker's yeast and beta-cyclodextrin |
Author: | Easton, Christopher J. Hughes, Christine Merricc M. Tiekink, Edward Richard Tom Savage, G. Paul Simpson, George W. |
Citation: | Tetrahedron Letters. 36:629-632 |
Publisher: | Pergamon Press |
Issue Date: | 1995 |
ISSN: | 0040-4039 |
School/Discipline: | School of Chemistry and Physics School of Chemistry and Physics : Chemistry |
Statement of Responsibility: | Christopher J. Easton, C. Merrîcc, M. Hughes, Edward R.T. Tiekink, G. Paul Savage, Gregory W. Simpson |
Abstract: | Contrary to recent reports, baker's yeast is not required for reactions of nitrile oxides with either ethyl cinnamate or 4-vinylpyridine to give isoxazolines. β-Cyclodextrin may alter the ratio of isomers isolated from the reactions of the cinnamate but only at concentrations of reactants much lower than those reported, and this effect is most likely due to selective product complexation rather than selective product formation. |
Rights: | Copyright © 1995 Published by Elsevier Ltd. |
DOI: | 10.1016/0040-4039(94)02321-2 |
Appears in Collections: | Chemistry publications |
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